GeneID: 291
Names
Common Name: | CTXND2 | Type: | Gene |
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Chromosome: | 1 (NC_000001.11) | Locus: | NR_148929.1 (CTXND2) |
HUGO Symbol: | CTXND2 | Full Name: | cortexin domain containing 2 |
Exons: | 2 | Introns: | 1 |
Description:
Cortexin domain containing 2 (CTXND2) is a long non-coding RNA (lncRNA). lncRNAs play a role in the regulation of gene expression. Cortexin is a neuron-specific membrane protein and variations in CTXND2 have been associated with neoplastic disease. A variation in this gene has been associated with acute chest syndrome (ACS) in cohorts with sickle cell disease. ACS is a form of acute lung injury caused by vaso-occlusion within the pulmonary microvasculature. Etiologies either trigger vaso-occlusion (e.g., infection, asthma, hypoventilation) or are a result of vaso-occlusion (e.g., bone marrow and fat emboli).
Synonyms: N/A
Comments:
N/A
Number of entries/variants: 1
IthaScore
Sequence Viewer
Publications / Origin
- Melton CW, Haynes J, Sickle acute lung injury: role of prevention and early aggressive intervention strategies on outcome., Clin. Chest Med., 27(3), 487-502, vii, 2006 PubMed
- Galarneau G, Coady S, Garrett ME, Jeffries N, Puggal M, Paltoo D, Soldano K, Guasch A, Ashley-Koch AE, Telen MJ, Kutlar A, Lettre G, Papanicolaou GJ, Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients., Blood , 122(3), 434-42, 2013 PubMed
- Ransohoff KJ, Wu W, Cho HG, Chahal HC, Lin Y, Dai HJ, Amos CI, Lee JE, Tang JY, Hinds DA, Han J, Wei Q, Sarin KY, Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma., Oncotarget, 8(11), 17586-17592, 2017 PubMed
A/A | Date | Curator(s) | Comments |
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1 | 2019-10-02 12:20:29 | The IthaGenes Curation Team | Created |